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Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Glucocorticoid and mineralocorticoid therapy effectively manage Congenital Adrenal Hyperplasia symptoms but have limitations.

People with reproductive, thyroid disorders, and type 2 diabetes can experience voice changes, but more research is needed to understand this better.

To diagnose Polycystic Ovarian Syndrome, two out of three signs—irregular periods, high male hormone levels, or cysts on the ovaries—are needed.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

Women with androgen excess, especially those with PCOS, have a much higher risk of heart disease and stroke.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

Hair loss can have various causes and treatments vary in effectiveness.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Congenital triangular alopecia and vitiligo can occur together, but treatment for one may not affect the other.

The book explains how excess male hormones can affect various conditions like Polycystic Ovary Syndrome and Cushing's disease.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Hair growth dysfunction involves various conditions with limited treatment options.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

The painting of an 18th-century Sicilian baroness shows she had hair loss, possibly due to ovarian issues, insulin resistance, or a specific type of tumor.

Hirsutism requires identifying the cause to choose the right treatment, which may include medications like oral contraceptives or dexamethasone.

Excess male hormones in postmenopausal women can cause health issues and increase the risk of heart disease and diabetes; treatment depends on the cause.

Some ovarian tumors can cause masculinization, and it's important to check for various causes when this symptom is present.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.